电解质
阳极
锂(药物)
材料科学
磷
碳化
化学工程
氧化物
电导率
离子电导率
无机化学
图层(电子)
氟化锂
纳米技术
化学
复合材料
冶金
电极
内分泌学
物理化学
工程类
医学
扫描电子显微镜
作者
Liang Xu,Xu Li,Qianxin Xiang,Shaojie Zhang,Yu Cao,Xinpeng Han,Yiming Zhang,Chaoyi Zhou,Yunhua Xu,Chong Mao,Weiyang Li,Jie Sun
出处
期刊:Nano Letters
[American Chemical Society]
日期:2022-11-15
卷期号:22 (23): 9335-9342
被引量:27
标识
DOI:10.1021/acs.nanolett.2c03038
摘要
By virtue of high theoretical capacity and appropriate lithiation potential, phosphorus is considered as a prospective next-generation anode material for lithium-ion batteries. However, there are some problems hampering its practical application, such as low ionic conductivity and serious volume expansion. Herein, we demonstrated an in situ preoxidation strategy to build a oxidation function layer at phosphorus particle. The oxide layer not only acted as a protective layer to prolong the storage time of phosphorus anode in air but also carbonized N-methyl pyrrolidone and poly (vinylidene fluoride), strengthening the interfacial interaction between phosphorus particles and binder. The oxide layer further induced the formation of a stable solid electrolyte interface with high lithium-ion conductivity. The oxidized P-CNT maintained high specific capacity of 1306 mAh g-1 and 89% capacity after 100 cycles, much higher than that of pristine P-CNT (17.1%). The strategy of in situ oxidation is facile and conducive to the practical application of phosphorus-based anodes.
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